ClinVar Miner

List of variants in gene SOS1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.2792-71C>T rs114521469 0.01505
NM_005633.4(SOS1):c.2511-98C>G rs41280637 0.01366
NM_005633.4(SOS1):c.510+59C>G rs180918477 0.00998
NM_005633.4(SOS1):c.2391-177T>A rs143611337 0.00701
NM_005633.4(SOS1):c.2168-251T>C rs114259556 0.00693
NM_005633.4(SOS1):c.1940+34T>C rs182069812 0.00675
NM_005633.4(SOS1):c.*3458A>C rs114232209 0.00673
NM_005633.4(SOS1):c.3346+261T>G rs143120043 0.00543
NM_005633.4(SOS1):c.865-49G>A rs149139868 0.00488
NM_005633.4(SOS1):c.3082-71G>A rs114702623 0.00480
NM_005633.4(SOS1):c.*3569T>C rs115465194 0.00421
NM_005633.4(SOS1):c.1202+286C>T rs75570154 0.00408
NM_005633.4(SOS1):c.1074+126C>T rs140589484 0.00397
NM_005633.4(SOS1):c.3082-331C>G rs141310875 0.00368
NM_005633.4(SOS1):c.3347-103A>G rs75266863 0.00365
NM_005633.4(SOS1):c.1941-34A>T rs143716812 0.00354
NM_005633.4(SOS1):c.2791+260T>A rs144826558 0.00322
NM_005633.4(SOS1):c.1859-40T>C rs55704100 0.00207
NM_005633.4(SOS1):c.864+35A>C rs56054777 0.00066
NM_005633.4(SOS1):c.2391-25T>C rs367873091 0.00042
NM_005633.4(SOS1):c.1489C>A (p.Arg497=) rs542368621 0.00018
NM_005633.4(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127 0.00017
NM_005633.4(SOS1):c.2966G>A (p.Arg989Lys) rs202043599 0.00016
NM_005633.4(SOS1):c.3706C>A (p.Pro1236Thr) rs727504636 0.00016
NM_005633.4(SOS1):c.3072C>T (p.Leu1024=) rs558386297 0.00013
NM_005633.4(SOS1):c.3330G>C (p.Ser1110=) rs146383828 0.00013
NM_005633.4(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736 0.00013
NM_005633.4(SOS1):c.3946C>G (p.His1316Asp) rs371024396 0.00013
NM_005633.4(SOS1):c.1269C>T (p.Asn423=) rs138459502 0.00010
NM_005633.4(SOS1):c.3418T>A (p.Leu1140Ile) rs375550588 0.00010
NM_005633.4(SOS1):c.244A>G (p.Ile82Val) rs397517157 0.00009
NM_005633.4(SOS1):c.2510+19C>G rs375675348 0.00009
NM_005633.4(SOS1):c.280A>G (p.Ile94Val) rs144757941 0.00009
NM_005633.4(SOS1):c.3322G>A (p.Asp1108Asn) rs199856844 0.00009
NM_005633.4(SOS1):c.511-47G>A rs754697135 0.00009
NM_005633.4(SOS1):c.511-48C>T rs200453620 0.00009
NM_005633.4(SOS1):c.864+26A>G rs369000327 0.00009
NM_005633.4(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026 0.00007
NM_005633.4(SOS1):c.1018C>T (p.Pro340Ser) rs190222208 0.00006
NM_005633.4(SOS1):c.2225T>C (p.Ile742Thr) rs767494615 0.00006
NM_005633.4(SOS1):c.929G>A (p.Arg310His) rs143481916 0.00006
NM_005633.4(SOS1):c.864+12A>C rs374379005 0.00005
NM_005633.4(SOS1):c.115G>A (p.Glu39Lys) rs375934353 0.00004
NM_005633.4(SOS1):c.1621T>C (p.Leu541=) rs371286473 0.00004
NM_005633.4(SOS1):c.1842G>A (p.Thr614=) rs143750479 0.00004
NM_005633.4(SOS1):c.2156G>C (p.Gly719Ala) rs200794965 0.00004
NM_005633.4(SOS1):c.2587C>A (p.Gln863Lys) rs141501083 0.00004
NM_005633.4(SOS1):c.3350A>G (p.Asn1117Ser) rs754314057 0.00004
NM_005633.4(SOS1):c.162A>G (p.Gln54=) rs763520126 0.00003
NM_005633.4(SOS1):c.3802G>A (p.Gly1268Ser) rs730881051 0.00003
NM_005633.4(SOS1):c.88-7T>A rs1416502603 0.00003
NM_005633.4(SOS1):c.1202+5A>G rs1021449471 0.00002
NM_005633.4(SOS1):c.3329C>T (p.Ser1110Leu) rs572955351 0.00002
NM_005633.4(SOS1):c.3384T>C (p.His1128=) rs1412775460 0.00002
NM_005633.4(SOS1):c.3836C>T (p.Thr1279Ile) rs758258471 0.00002
NM_005633.4(SOS1):c.3838C>A (p.Gln1280Lys) rs548519280 0.00002
NM_005633.4(SOS1):c.396A>T (p.Ala132=) rs727505385 0.00002
NM_005633.4(SOS1):c.899G>A (p.Arg300Gln) rs754374236 0.00002
NM_005633.4(SOS1):c.1458A>G (p.Ala486=) rs772746896 0.00001
NM_005633.4(SOS1):c.1848T>C (p.His616=) rs1344852617 0.00001
NM_005633.4(SOS1):c.1863C>T (p.Pro621=) rs759125551 0.00001
NM_005633.4(SOS1):c.1995T>C (p.Asn665=) rs779262456 0.00001
NM_005633.4(SOS1):c.2728G>C (p.Asp910His) rs369277679 0.00001
NM_005633.4(SOS1):c.2739G>A (p.Lys913=) rs997339872 0.00001
NM_005633.4(SOS1):c.2868A>C (p.Ile956=) rs758834690 0.00001
NM_005633.4(SOS1):c.2998A>T (p.Ser1000Cys) rs730881031 0.00001
NM_005633.4(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934 0.00001
NM_005633.4(SOS1):c.3189T>C (p.Ile1063=) rs576812416 0.00001
NM_005633.4(SOS1):c.3391+3T>C rs761579423 0.00001
NM_005633.4(SOS1):c.350T>G (p.Val117Gly) rs201085754 0.00001
NM_005633.4(SOS1):c.3552T>G (p.Pro1184=) rs200485215 0.00001
NM_005633.4(SOS1):c.3801C>T (p.His1267=) rs747676700 0.00001
NM_005633.4(SOS1):c.3900A>G (p.Gln1300=) rs1343754754 0.00001
NM_005633.4(SOS1):c.429G>A (p.Lys143=) rs773264070 0.00001
NM_005633.4(SOS1):c.643T>C (p.Tyr215His) rs730881039 0.00001
NM_005633.4(SOS1):c.675T>G (p.Val225=) rs371482290 0.00001
NM_005633.4(SOS1):c.726A>G (p.Val242=) rs1378914590 0.00001
NM_005633.4(SOS1):c.798A>C (p.Thr266=) rs756044708 0.00001
NM_005633.4(SOS1):c.834A>G (p.Leu278=) rs1301517846 0.00001
NM_005633.4(SOS1):c.984C>T (p.Gly328=) rs778223456 0.00001
NM_005633.3(SOS1):c.2511-9dup rs727503436
NM_005633.4(SOS1):c.*12C>T rs1057522437
NM_005633.4(SOS1):c.*8T>C rs1057521160
NM_005633.4(SOS1):c.1203-17C>G rs1553356202
NM_005633.4(SOS1):c.1203-25AAT[3] rs1553356212
NM_005633.4(SOS1):c.1203-8T>C rs1669853901
NM_005633.4(SOS1):c.1428G>A (p.Gly476=) rs902127095
NM_005633.4(SOS1):c.1434A>T (p.Pro478=) rs368495902
NM_005633.4(SOS1):c.1491A>G (p.Arg497=) rs1432437086
NM_005633.4(SOS1):c.1707G>A (p.Leu569=) rs1479407572
NM_005633.4(SOS1):c.1859-5_1859-3del rs1171459346
NM_005633.4(SOS1):c.1987A>G (p.Ile663Val) rs730881024
NM_005633.4(SOS1):c.2063+44T>C rs111576630
NM_005633.4(SOS1):c.2064-20A>T rs756707478
NM_005633.4(SOS1):c.213+14_213+16del rs768872084
NM_005633.4(SOS1):c.2168-42_2168-39del rs544376690
NM_005633.4(SOS1):c.2510+254dup rs113164980
NM_005633.4(SOS1):c.2510+268del rs113164980
NM_005633.4(SOS1):c.2511-13_2511-9del rs727503436
NM_005633.4(SOS1):c.2511-252_2511-251insTAT rs200649886
NM_005633.4(SOS1):c.2674-134del rs1425390621
NM_005633.4(SOS1):c.2791+11C>G rs1057521862
NM_005633.4(SOS1):c.3195T>C (p.Tyr1065=) rs1280224224
NM_005633.4(SOS1):c.3322G>C (p.Asp1108His) rs199856844
NM_005633.4(SOS1):c.3346+134_3346+136del rs200403937
NM_005633.4(SOS1):c.3511-133A>G rs193223219
NM_005633.4(SOS1):c.3511-14_3511-10del rs760713912
NM_005633.4(SOS1):c.3511-18A>T rs760383259
NM_005633.4(SOS1):c.3601C>T (p.Arg1201Trp) rs752395541
NM_005633.4(SOS1):c.3620C>G (p.Pro1207Arg) rs730881025
NM_005633.4(SOS1):c.3709C>A (p.Pro1237Thr) rs371408734
NM_005633.4(SOS1):c.3948C>T (p.His1316=) rs1399242305
NM_005633.4(SOS1):c.3996T>C (p.Ser1332=) rs1057522315
NM_005633.4(SOS1):c.511-9_511-6del rs986512473
NM_005633.4(SOS1):c.654A>G (p.Glu218=) rs2124603600
NM_005633.4(SOS1):c.822T>C (p.Ser274=) rs1057522964
NM_005633.4(SOS1):c.865-344A>T rs116259655
NM_005633.4(SOS1):c.976-5dup rs771586560

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